IRF-2 haploinsufficiency causes enhanced imiquimod-induced psoriasis-like skin inflammation

You are here:
  • Main
  • Publications
  • 2017
  • IRF-2 haploinsufficiency causes enhanced imiquimod-induced psoriasis-like skin inflammation
< All Topics

Publication:

Journal of Dermatological Science
Volume 90, Issue 1, April 2018, Pages 35-45

https://doi.org/10.1016/j.jdermsci.2017.12.014

Author(s):

Makiko Kawaguchi, Tomonori Oka, Makoto Sugaya, Hiraku Suga, Takayuki Kimura, Sohshi Morimura, Hideki Fujita, Shinichi Sato

Quansys Products Used:

Q-Plex Custom Array

Abstract:

Backgrounds
IFN regulatory factor (IRF)-2 is one of the potential susceptibility genes for psoriasis, but how this gene influences psoriasis pathogenesis is unclear. Topical application of imiquimod (IMQ), a TLR7 ligand, induces psoriasis-like skin lesions in mice.

Objective
The aim of this study was to investigate whether IRF-2 gene status would influence severity of skin disease in IMQ-treated mice.

Methods
Imiquimod-induced psoriasis-like skin inflammation was assessed by clinical findings, histology, and cytokine expression. The effects of imiquimod or IFN on peritoneal macrophages were analyzed in vitro.

Results
IMQ-induced skin inflammation assessed by clinical findings and histology was more severe in IRF-2+/− mice than in wild-type mice. In inflamed skin, mRNA expression levels of tumor necrosis factor (TNF)-α, IL-12/23p40, IL-17A, and IL-22 were significantly elevated in IRF-2+/− mice compared to wild-type mice. Stimulation of peritoneal macrophages by IMQ significantly increased mRNA levels of TNF-α, IL-12/23p40, IL-23p19, IL-12p35, and IL-36. Interestingly, macrophages from IRF-2+/− mice expressed higher levels of TNF-α, IL-12/23p40, and IL-36 compared to those from wild-type mice 24 h after stimulation, while they expressed similar levels of IL-12p35 and IL-23p19. Moreover, elevated mRNA expression of inducible nitric oxide synthase was observed only in IMQ-stimulated macrophages derived from IRF-2+/− mice, which correlated with angiogenesis in IMQ-treated ears of IRF-2+/− mice.

Conclusions
These results suggest that IRF-2 haploinsufficiency creates heightened biologic responses to IFN-α that phenotypically lead to enhanced angiogenesis and psoriasis-like inflammation within skin

Next Leukoreduction of packed red blood cells attenuates proinflammatory properties of storage-derived microvesicles